α -平滑肌肌动蛋白(αSMA)和诱导型一氧化氮合酶(iNOS)在口腔鳞状细胞癌(OSCC)中的价值:一种免疫组织化学方法用于肿瘤间质分类和临床病理参数

Heba E.M. Youssef , Basant Hamdy AbouZaid
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引用次数: 0

摘要

目的口腔鳞状细胞癌(OSCC)的侵袭行为不仅是一个以癌细胞为中心的问题,而且还受肿瘤间质的影响。肿瘤相关成纤维细胞(CAFs)是肿瘤基质中最丰富的可指导肿瘤发生的成分。α-平滑肌肌动蛋白(α-SMA)在间质cas中的表达与高侵袭性肿瘤行为和不良预后有关。诱导型一氧化氮合酶(Inducible nitric oxide synthase, iNOS)是在各种刺激下产生自由基、一氧化氮的主要酶之一。其表达的增加显示出几种促肿瘤作用。本研究旨在探讨α-SMA和iNOS在OSCC中表达与肿瘤基质类型和肿瘤细胞分化程度的关系。方法采用抗α- sma和抗inos免疫组织化学染色方法对32例OSCC档案标本进行染色。根据α-SMA阳性面积与肿瘤浸润淋巴细胞密度之比进行基质分类。半定量评价iNOS免疫组化评分。最后,观察基质类型、iNOS表达与不同临床病理参数的相关性。结果高组织病理分级与高间质分级呈正相关(P = 0.02)。此外,间质类型的增加与晚期临床分期(P = 0.001)和淋巴结受累(P = 0.05)显著相关。iNOS表达与肿瘤组织病理分级恶化(P = 0.008)及临床分期(P = 0.01)相关。结论结合基质类型和iNOS表达的评估可以提供更全面的OSCC肿瘤微环境特征,而不仅仅是单一参数的肿瘤或基质特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Value of alpha smooth muscle actin (αSMA) and inducible nitric oxide synthase (iNOS) in oral squamous cell carcinoma (OSCC): An immunohistochemical approach to tumor stroma categorization and clinicopathological parameters

Objectives

The aggressive behavior of oral squamous cell carcinoma (OSCC) is not only a cancer-cell centered issue, but also affected by tumor stroma. Cancer-associated fibroblasts (CAFs) are the most abundant component of tumor stroma that can direct tumorigenesis. Alpha smooth muscle actin (α-SMA) expression by stromal CAFs is linked to higher aggressive tumor behavior and poor prognosis. Inducible nitric oxide synthase (iNOS) is one of the main enzymes producing the free radical, nitric oxide in response to various stimuli. Its increased expression revealed several pro-tumorigenic effects. This study was undertaken to address the expression of α-SMA and iNOS in OSCC in relation to tumor stroma type and degree of tumor cell differentiation.

Methodology

Thirty-two archival specimens of OSCC were stained immunohistochemically with anti-α-SMA and anti-iNOS. Stromal categorization was performed according to the ratio between α-SMA positive areas and the density of tumor infiltrating lymphocytes. The immunohistochemical score of iNOS was evaluated semi-quantitatively. Finally, correlations between stroma category, iNOS expression and different clinicopathological parameters were performed.

Results

Our results revealed a significant positive correlation between advanced histopathologic grade and the higher stromal category (P = 0.02). Additionally, increased stroma category was significantly associated with advanced clinical stage (P = 0.001) and nodal involvement (P = 0.05). Likewise, iNOS expression was significantly correlated with worsened histopathological grade (P = 0.008) and clinical stage of tumors (P = 0.01).

Conclusions

Combining the assessment of stroma category and iNOS expression offers a more comprehensive tumor microenvironment profile in OSCC, surpassing single-parameter approaches focused solely on tumor or stromal characteristics.
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